Canonical Allele Identifier: CA891840566

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894079_87894080delinsAT , CM000672.2:g.87894079_87894080delinsAT	GRCh38
NC_000010.10:g.89653836_89653837delinsAT , CM000672.1:g.89653836_89653837delinsAT	GRCh37
NC_000010.9:g.89643816_89643817delinsAT	NCBI36
NG_007466.2:g.35641_35642delinsAT , LRG_311:g.35641_35642delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.134_135delinsAT	ENSP00000514759.2:p.Val45Asp
ENST00000710265.1:c.134_135delinsAT	ENSP00000518161.1:p.Val45Asp
ENST00000472832.3:c.134_135delinsAT	ENSP00000483066.2:p.Val45Asp
ENST00000688158.2:n.899+13641_899+13642delinsAT
ENST00000688922.2:c.134_135delinsAT	ENSP00000508742.2:p.Val45Asp
ENST00000700021.1:c.134_135delinsAT	ENSP00000514757.1:p.Val45Asp
ENST00000700022.1:c.134_135delinsAT	ENSP00000514758.1:p.Val45Asp
ENST00000706954.1:c.134_135delinsAT	ENSP00000516674.1:p.Val45Asp
ENST00000706955.1:c.*169_*170delinsAT	ENSP00000516675.1:n.*169_*170delinsAT
ENST00000686459.1:c.134_135delinsAT	ENSP00000508909.1:p.Val45Asp
ENST00000688158.1:c.*275+13641_*275+13642delinsAT	ENSP00000509254.1:n.*275+13641_*275+13642delinsAT
ENST00000688308.1:c.134_135delinsAT	ENSP00000508752.1:p.Val45Asp
ENST00000688922.1:c.3_4delinsAT
ENST00000693560.1:c.653_654delinsAT	ENSP00000509861.1:p.Val218Asp
ENST00000371953.8:c.134_135delinsAT MANE Select	ENSP00000361021.3:p.Val45Asp
ENST00000371953.7:c.134_135delinsAT	ENSP00000361021.3:p.Val45Asp
ENST00000462694.1:n.136_137delinsAT
ENST00000610634.1:c.32_33delinsAT	ENSP00000477517.1:p.Val11Asp
NM_000314.5:c.134_135delinsAT	NP_000305.3:p.Val45Asp
NM_000314.6:c.134_135delinsAT	NP_000305.3:p.Val45Asp
NM_001304717.2:c.653_654delinsAT	NP_001291646.2:p.Val218Asp
NM_001304718.1:c.-572_-571delinsAT	NP_001291647.1:n.-572_-571delinsAT
XM_006717926.2:c.134_135delinsAT	XP_006717989.1:p.Val45Asp
XM_011539981.1:c.134_135delinsAT	XP_011538283.1:p.Val45Asp
XM_011539982.1:c.68+13641_68+13642delinsAT	XP_011538284.1:n.68+13641_68+13642delinsAT
XR_945789.1:n.846_847delinsAT
XR_945790.1:n.846_847delinsAT
XR_945791.1:n.846_847delinsAT
NM_000314.7:c.134_135delinsAT	NP_000305.3:p.Val45Asp
NM_001304717.5:c.653_654delinsAT	NP_001291646.4:p.Val218Asp
NM_001304718.2:c.-572_-571delinsAT	NP_001291647.1:n.-572_-571delinsAT
NM_000314.8:c.134_135delinsAT MANE Select	NP_000305.3:p.Val45Asp